To meet the needs of clinical medicine, bone tissue engineering is developing dynamically. Scaffolds for bone healing might be used as solid, preformed scaffolding materials, or through the injection of a solidifiable precursor into the defective tissue. There are miscellaneous biomaterials used to stimulate bone repair including ceramics, metals, naturally derived polymers, synthetic polymers, and other biocompatible substances. Combining ceramics and metals or polymers holds promise for future cures as the materials complement each other. Further research must explain the limitations of the size of the defects of each scaffold, and additionally, check the possibility of regeneration after implantation and resistance to disease. Before tissue engineering, a lot of bone defects were treated with autogenous bone grafts. Biodegradable polymers are widely applied as porous scaffolds in bone tissue engineering. The most valuable features of biodegradable polyurethanes are good biocompatibility, bioactivity, bioconductivity, and injectability. They may also be used as temporary extracellular matrix (ECM) in bone tissue healing and regeneration. Herein, the current state concerning polyurethanes in bone tissue engineering are discussed and introduced, as well as future trends.
The thermal properties of chitosan and hydroxyapatite (HAp)-crosslinked polyurethanes (PU) prepared in a two-step bulk polymerization were investigated. Synthesis of PU was carried out using 1,6-hexamethylene diisocyanate, poly(ethylene glycol) 2000 and dibutyltin dilaurate as a catalyst. Various molar ratios of chitosan and 1,4-butanediol were applied, and the effects of incorporating different HAp amounts and the chitosan-to-BDO ratio were studied. It was found that the thermal properties of PU materials depend on polysaccharides and bioceramics load, which was confirmed by differential scanning calorimetry and thermogravimetry. The glass transition temperature increases with increasing chitosan fraction. Similarly, the onset temperature of degradation increased with chitosan addition. On the other hand, the presence of ceramics did not show a significant impact on the thermal properties of PU composites. Successful polymerization and chain extension of the isocyanate groups with hydroxyl moieties from chitosan and HAp were confirmed by Fourier transform infrared spectroscopy, and the morphology was examined using scanning electron microscopy.
In this study, modified polyurethanes (PUs) with starch and magnetite were synthesized in the form of scaffolds for potential applications in orthopedics. Polyurethanes were synthesized using a one-step method. PU synthesis was carried out using poly(ε-caprolactone) 2000 as soft segments and 4,4
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-methylenediphenyl diisocyanate (MDI). Various molar ratios of starch and 1,5-pentanediol (PDO) as crosslinker/chain extender were applied, and the effects of incorporating different amounts of magnetite, as well as the role of PDO to starch ratio, were studied. The use of the additive in the form of magnetic particles was to feature the polyurethane materials for use in hyperthermia. The prepared polyurethanes were investigated using Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), thermogravimetry (TG), and dynamic mechanical analysis (DMA) methods. Scanning electron microscopy (SEM)/energy-dispersive X-ray spectroscopy (EDX) analysis and preliminary bioactivity assessment were also performed. The addition of magnetic particles did not cause significant changes in the properties of the obtained materials compared to starch. The tested materials have the potential to be used to fill or replace bone defects in orthopedics, where they can undergo hyperthermia treatment.
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